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Summary Literature (0)
DOID:0111091 - Fanconi anemia complementation group I

Disease Ontology Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCI gene on chromosome 15q26.

Synonyms: FANCI

Xenbase Genes : fanci

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012186 - Fanconi anemia complementation group I


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), Fanconi anemia (is_a)